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用于在炎症性肠病中实现姜黄素结肠递送的pH敏感纳米颗粒。

pH-sensitive nanoparticles for colonic delivery of curcumin in inflammatory bowel disease.

作者信息

Beloqui Ana, Coco Régis, Memvanga Patrick B, Ucakar Bernard, des Rieux Anne, Préat Véronique

机构信息

Université catholique de Louvain, Louvain Drug Research Institute, Advanced Drug Delivery and Biomaterials, 1200 Brussels, Belgium.

Université catholique de Louvain, Louvain Drug Research Institute, Advanced Drug Delivery and Biomaterials, 1200 Brussels, Belgium; University of Kinshasa, Faculty of Pharmaceutical Sciences, Laboratoire de Pharmacie galénique, BP 212 Kinshasa XI,Democratic Republic of the Congo.

出版信息

Int J Pharm. 2014 Oct 1;473(1-2):203-12. doi: 10.1016/j.ijpharm.2014.07.009. Epub 2014 Jul 8.

Abstract

Nano-scaled particles have been found to preferentially accumulate in inflamed regions. Local delivery of anti-inflammatory drugs loaded in nanoparticles to the inflamed colonic site is of great interest for inflammatory bowel disease (IBD) treatment. Curcumin (CC) is an anti-inflammatory local agent, which presents poor ADME properties. Hence, we evaluated, both in vitro and in vivo, the local delivery of CC using pH-sensitive polymeric nanoparticles (NPs) combining both poly(lactide-co-glycolide) acid (PLGA) and a polymethacrylate polymer (Eudragit(®) S100). CC-NPs significantly enhanced CC permeation across Caco-2 cell monolayers when compared to CC in suspension. CC-NPs significantly reduced TNF-α secretion by LPS-activated macrophages (J774 cells). In vivo, CC-NPs significantly decreased neutrophil infiltration and TNF-α secretion while maintaining the colonic structure similar to the control group in a murine DSS-induced colitis model. Our results support the use of nanoparticles made of PLGA and Eudragit(®) S100 combination for CC delivery in IBD treatment.

摘要

已发现纳米级颗粒会优先在炎症区域积聚。将负载抗炎药物的纳米颗粒局部递送至发炎的结肠部位,对于炎症性肠病(IBD)的治疗具有重大意义。姜黄素(CC)是一种抗炎局部药物,但其吸收、分布、代谢和排泄(ADME)特性较差。因此,我们在体外和体内评估了使用结合聚(丙交酯-共-乙交酯)酸(PLGA)和聚甲基丙烯酸酯聚合物(尤特奇(®)S100)的pH敏感聚合物纳米颗粒(NPs)进行CC的局部递送。与悬浮状态的CC相比,CC-NPs显著增强了CC跨Caco-2细胞单层的渗透。CC-NPs显著降低了脂多糖激活的巨噬细胞(J774细胞)分泌的肿瘤坏死因子-α(TNF-α)。在体内,在小鼠葡聚糖硫酸钠(DSS)诱导的结肠炎模型中,CC-NPs显著减少了中性粒细胞浸润和TNF-α分泌,同时保持结肠结构与对照组相似。我们的结果支持使用由PLGA和尤特奇(®)S100组合制成的纳米颗粒在IBD治疗中递送CC。

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